acrocephalosyndactyly 是什么意思，中文意思 | 尖颅并指（趾）畸形英文怎么说医学英语中英文词汇翻译

Apert syndrome: clinical and radiographic features and case report

[PDF] from pucrs.brFP Varoli, KCP Santos… - … Ciência (Journal of …, 2011 - revistaseletronicas.pucrs.br
... usp.br Abstract Purpose: Apert syndrome is a rare type I acrocephalosyndactyly
syndrome characterized by craniosynostosis, severe syndactyly of the hands and
feet, and dysmorphic facial features. Presents autosomal dominant ...
Cited by 1 - Related articles - All 3 versions

Apert 症候群 (特集 Craniosynostosis・先天性頭蓋顔面骨異常の治療)--(症候群性頭蓋縫合早期癒合症)

宮脇剛司 - ペパーズ, 2011 - ci.nii.ac.jp
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Pfeiffer 症候群, Saethre-Chotzen 症候群, クローバーリーフ頭蓋 (特集 Craniosynostosis・先天性頭蓋顔面骨異常の治療)--(症候群性頭蓋縫合早期癒合症)

藤本卓也… - ペパーズ, 2011 - ci.nii.ac.jp
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Microdeletions of chromosome 7p21, including TWIST1, associated with significant microcephaly, facial dysmorphism, and short stature

A Busche, LM Graul-Neumann, C Zweier… - European Journal of …, 2011 - Elsevier
... syndrome, TWIST1, deletion 7p21, blepharophimosis-ptosis-40 epicanthus inversus syndrome
41 42 43 44 45 46 47 48 49 50 51 52 MA NUSCRIPTACCEPTED ACCEPTED MANUSCRIPT
3 53 1. Introduction 54 Saethre-Chotzen syndrome or acrocephalosyndactyly type III ...
All 2 versions

[HTML] An Insight Into The Spectrum Of Apert Syndrome–A Case Study

[HTML] from ispub.comR Narang, S Sandhu, S Padda, J Sandhu… - The Internet Journal of …, 2011 - ispub.com
... 1. Acrocephalosyndactyly is a variant of craniosynostosis which is characterized by acrocephaly
and syndactyly of hands and feet often combined with anomalies of other organs. Some
investigators state that 4.5 percent of all craniosynostosis represent Apert syndrome. ...
Cached

Apert syndrome: clinical and radiographic features and case report

[PDF] from pucrs.brFP Varoli, KCP Santos… - … Ciência (Journal of …, 2011 - revistaseletronicas.pucrs.br
... usp.br Abstract Purpose: Apert syndrome is a rare type I acrocephalosyndactyly
syndrome characterized by craniosynostosis, severe syndactyly of the hands and
feet, and dysmorphic facial features. Presents autosomal dominant ...
Cited by 1 - Related articles - All 3 versions

Apert 症候群 (特集 Craniosynostosis・先天性頭蓋顔面骨異常の治療)--(症候群性頭蓋縫合早期癒合症)

宮脇剛司 - ペパーズ, 2011 - ci.nii.ac.jp
Cached

Pfeiffer 症候群, Saethre-Chotzen 症候群, クローバーリーフ頭蓋 (特集 Craniosynostosis・先天性頭蓋顔面骨異常の治療)--(症候群性頭蓋縫合早期癒合症)

藤本卓也… - ペパーズ, 2011 - ci.nii.ac.jp
Cached

Microdeletions of chromosome 7p21, including TWIST1, associated with significant microcephaly, facial dysmorphism, and short stature

A Busche, LM Graul-Neumann, C Zweier… - European Journal of …, 2011 - Elsevier
... syndrome, TWIST1, deletion 7p21, blepharophimosis-ptosis-40 epicanthus inversus syndrome
41 42 43 44 45 46 47 48 49 50 51 52 MA NUSCRIPTACCEPTED ACCEPTED MANUSCRIPT
3 53 1. Introduction 54 Saethre-Chotzen syndrome or acrocephalosyndactyly type III ...
All 2 versions

[HTML] An Insight Into The Spectrum Of Apert Syndrome–A Case Study

[HTML] from ispub.comR Narang, S Sandhu, S Padda, J Sandhu… - The Internet Journal of …, 2011 - ispub.com
... 1. Acrocephalosyndactyly is a variant of craniosynostosis which is characterized by acrocephaly
and syndactyly of hands and feet often combined with anomalies of other organs. Some
investigators state that 4.5 percent of all craniosynostosis represent Apert syndrome. ...
Cached

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[HTML] An Insight Into The Spectrum Of Apert Syndrome–A Case Study

[HTML] An Insight Into The Spectrum Of Apert Syndrome–A Case Study